A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131351



Internal ID21483670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176393415..176393415hg38UCSC Ensembl
chr5:175820416..175820416hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624609
Supporting Variants
SamplesHG03732
Known GenesCLTB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131351
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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